Device for osteosyntheses or arthrodesis of two-bone parts, in particular of the hand and/or foot

ABSTRACT

In one embodiment, the present invention is a method of arthrodesis or osteosyntheses of a first bone part and a second bone part, including the steps of positioning a first fixation zone of an implant in the first bone part and a second fixation zone of the implant in the second bone part, both the first and second zones made of shape-memory material and, prior to positioning the bone parts, are in an inner position; and while the first fixation zone is within the first bone part and the second fixation zone is within the second bone part, fixating the respective first and second fixation zones within the respective bone parts through shape-memory action at body temperature.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 16/020,005, filed Jun. 27, 2018, which is a continuation of U.S. application Ser. No. 15/292,955, now U.S. Pat. No. 10,022,167, filed Oct. 13, 2016, which is a continuation of U.S. application Ser. No. 13/896,894, now U.S. Pat. No. 9,492,215, filed May 17, 2013, which is a continuation of U.S. application Ser. No. 11/911,405, now U.S. Pat. No. 8,475,456, filed Mar. 17, 2008, which is a US national phase of PCT Publication PCT/FR2006/050345, filed 12 Apr. 2006, published 19 Oct. 2006 as WO2006/109004, and claiming the priority of French Application No. 0550957, filed Apr. 14, 2005, the entire disclosures of each of which are herewith incorporated by reference herein.

FIELD OF THE INVENTION

The invention relates to the technical field of orthopaedic implants, particularly for arthrodesis and osteosyntheses.

It may be recalled that the object of an arthrodesis is to obtain very good stability both primary and secondary, and to place, or to maintain, in compression, two bone parts or bone fragments that should be consolidated. Stability is a critical factor for obtaining consolidation, while minimizing the attendant problems such as pain, swelling, etc. The compressive action serves to consolidate the osteotomy more rapidly in the position selected by the surgeon during the operation.

Various technical solutions have been proposed for carrying out an arthrodesis, particularly in the foot, the hand, the wrist, etc. Mention can be made, for example, of basic staples without shape memory which do not produce a compression, as opposed to memory staples which serve to place the two bone parts to be consolidated in compression, which corresponds to the objective.

However, to obtain satisfactory stability, it is necessary to place two, or even three staples, in different planes. This increases the dimensions considerably, thereby limiting applications (metacarpo-phalangeal joint, for example).

Extramedullary plates and screws have also been proposed, requiring an alternatively large dimension. In this respect, their miniaturization is difficult to conceive, because this could raise problems of strength and stiffness. Some types of screws can be used in intramedullary osteosynthesis, but they raise positioning difficulties (passage through the pad in particular).

Use can also be made of pins which have a smaller size. However, the stability obtained is unsatisfactory and it is necessary to withdraw them.

Intramedullary nails are also known, but they require supplementary stapling in order to prevent the bone parts to be joined from rotating relative to each other.

OBJECT OF THE INVENTION

It is the object of the invention to remedy these drawbacks simply, safely, effectively and efficiently.

The problem that the invention proposes to solve is to permit the fixation of two bone parts to one another, rigidly with dynamic and retentive compression, in order to obtain a reliable and rapid osteosynthesis.

SUMMARY OF THE INVENTION

To solve such a problem, an intramedullary arthrodesis element has been designed and developed which consists of a body with an elongated shape having, in succession, from one of its ends, a fixation zone cooperating with one of the bone parts to be immobilized, a median zone suitable for withstanding shear and bending stresses, and a fixation zone in the other bone part to be immobilized, each of the fixation zones being profiled and made from a material suitable for enabling introduction into the bone parts without a finger- or toe-tip approach, followed by a fixation in the bone parts, while avoiding any rotational movement, withstanding the tensile stresses, and maintaining a compressive force.

The invention has a particularly advantageous application, which can however not be considered as limiting, for the preparation of arthrodesis in the proximal and median phalanges, for proximal interphalangeal joints and distal interphalangeal joints, in the hand or foot.

To solve the problem of taking account of the anatomy, and particularly of the internal shrinkage of the bone, the median zone is linked to at least one of the fixation zones by a connecting zone.

To solve the problem of permitting implantation of the element followed by compression of the bone fragments, the fixation zones are made from a shape-memory material to be deformed by thermal and/or mechanical action.

To produce the fixation zones, which may be identical or not, various technical solutions are feasible, according in particular to the type of arthrodesis performed and the joints to be treated.

For Example:

one of the fixation zones has two tabs or wings separable under the action of the shape memory;

one of the fixation zones has a tab or rod which can be curved under the action of the shape memory;

one of the fixation zones has, in its thickness, a slot for permitting deformation by elasticity, or memory, under the action of the shape memory.

In one embodiment, the overall body has a flat cross-section.

BRIEF DESCRIPTION OF THE DRAWING

The invention is described below in greater detail in conjunction with the figures of the drawings appended hereto in which:

FIG. 1 is a schematic plan view showing the placement of the intramedullary arthrodesis element of the invention between a proximal phalange and a median phalange to consolidate the proximal interphalangeal joint;

FIG. 2 is a plan view of an embodiment of the arthrodesis element at the time of its introduction;

FIG. 3 is a view corresponding to FIG. 2 showing the arthrodesis element after its implant to produce the compression;

FIG. 4 shows the placement of the element of the invention in a toe.

SPECIFIC DESCRIPTION

The arthrodesis element of the invention consists of an elongated body 1. Each of the ends of the body 1 is conformed to produce a fixation zone 1 a linked to a fixation zone 1 b.

Between the two fixation zones 1 a and 1 b, at least one median zone 1 c is formed capable of withstanding shear and bending stresses. In general, the shear and bending stresses are applied to the bone site to be consolidated. The shape of this median zone 1 c is adapted to the internal shape of the bone. Its length is determined in order to allow a slight offset in the centering.

For information, and in a non-limiting manner, this median zone may have a rectangular cross-section measuring about 2 to 3 mm*1 to 1.5 mm and a length of about 3 to 5 mm for the foot and the hand.

The fixation zones 1 a and 1 b are conformed to prevent any rotational movement, resist tension, and maintain manual compression applied at the time of the implant by the surgeon in order to reduce the site. To obtain this result, the fixation zones 1 a and 1 b are made from a shape-memory material to be deformed by thermal action (tepid memory) or mechanical action (superelasticity) (see U.S. Pat. No. 5,958,159). The goal, in the fixation zones, considering their profile on the one hand and the type of material on the other, is to permit an introduction into the bone parts, particularly dorsally without a finger- or toe-tip approach, on the one hand, and to produce a fixation in the bone portion in order to obtain or to maintain the desired compressive force, on the other. The fixation zones 1 a and 1 b are identical or not, according to the type of bone and its morphology.

Depending on the type of arthrodesis performed, that is, the type of interphalangeal joint to be consolidated for example, the fixation zones 1 a and 1 b may have different embodiments.

For example, one of the fixation zones 1 a has two tabs or wings that are separable under a thermal action for example. Otherwise, these fixation zones 1 a may have a single tab or rod which can be curved under the action of a memory of the component material. Otherwise, the fixation zone 1 b has, in its thickness, a slot to permit deformation by elasticity, under thermal action for example, and to maintain the position by pressing on the length of the bone.

According to another feature of the invention, to take account of the anatomy of the various phalanges for example, that is the internal shrinkage of the bone (hourglass shape), the median zone 1 c is linked to at least one of the fixation zones 1 b by a thinner connecting zone 1 d.

Reference can be made to the figures of the drawings which show an embodiment of an intramedullar arthrodesis element.

In this embodiment, the body 1 has, at one of its ends, a fixation zone 1 a in the form of two tabs or wings 1 a 1 1 a 2. This fixation zone 1 a is prolonged by a median zone 1 c of generally substantially triangular shape in a plan view. The median zone 1 c is connected to the other end fixation zone 1 b by a connecting zone 1 d having a generally rectangular shape in a plan view. The fixation zone 1 b has, in its thickness, a slot of generally oblong shape 1 b 1.

Reference can be made to FIG. 2 which shows the element at the time of its introduction, that is before separation of the tabs 1 a 1 and 1 a 2, and the opening of the slot 1 b 1. For example, this configuration is obtained when the overall element is subject to a temperature much lower than that of the human body for example. Conversely, after implantation (FIG. 3), under the effect of body heat, the tabs 1 a 1 and 1 a 2 separate, in the same way as the slot 1 b 1, concomitantly causing a deformation of the fixation zone 1 b.

It should be noted that the profile of the median zone 1 c prevents penetration when the site is reclosed.

In an alternative embodiment, the connecting zone 1 d can be split to benefit from a swelling effect by shape memory and strengthening of the anchoring in the diaphyseal zone.

It should be recalled that the inventive element is ideal for the treatment of the hammer- or claw-toe syndrome, by performing an arthrodesis in the phalanges P1 and P2 on the radii 2 to 5, while observing that such applications must not be considered as limiting, by means of essentially dimensional adjustments (finger reimplants, arthrodesis of the distal interphalangeal joint and of the proximal interphalangeal joint of the hand, and the arthrodesis of the big toe).

Obviously, the entire arthrodesis element of the invention may have constructive features suitable for improving the fixation and compression in particular.

For example:

notches on the tabs on one of the sides for better fixation in the ethmoid bone;

wavy tabs implanted (straight before implant) to permit shortening and hence an additional compression of the arthrodesis site compared with a simple fixation;

a tapered central zone to avoid undesirable penetration of the implant at the time when the site is to be closed.

For information, the memory used is preferably a tepid memory, so that heating is unnecessary because of the lack of access. The opening begins at above 15 to 20° C. and stops at about 30 to 35° C.

The operating technique remains conventional. 

The invention claimed is:
 1. An intramedullary implant for implantation into first and second bone parts, the implant comprising: a median zone having a first end, a second end opposite the first end, and a plurality of side faces between the first and the second ends, the plurality of side faces converging toward the second end, the first end defining an abutment; a first fixation zone extending from the median zone and including first and second legs extending from the abutment, the first and second legs defining a V-shaped gap extending from the abutment, each of the first and second legs including a projection, the V-shaped gap having a first distance adjacent the median zone and a second distance away from the median zone, the first distance being less than the second distance; and a second fixation zone extending from the median zone.
 2. The intramedullary implant of claim 1, wherein the first end has a first width and the second end has a second width, the first width being greater than the second width.
 3. The intramedullary implant of claim 1, wherein the first end has a first cross-sectional dimension and the second end has a second cross-sectional section, the first cross-sectional dimension being greater than the second cross-sectional dimension.
 4. The intramedullary implant of claim 1, wherein the first fixation extends from the first end and the second fixation zone extends from the second end.
 5. The intramedullary implant of claim 1, wherein the second fixation zone defines an opening therethrough.
 6. The intramedullary implant of claim 1, wherein the median zone includes an intermediate face between the plurality of side faces and the abutment.
 7. The intramedullary implant of claim 6, wherein the intramedullary implant defines a longitudinal axis and the intermediate face is parallel to the longitudinal axis.
 8. The intramedullary implant of claim 1, wherein the first fixation zone extends from the median zone in a proximal direction.
 9. The intramedullary implant of claim 8, wherein the second fixation zone extends in a distal direction opposite the proximal direction.
 10. An intramedullary implant for implantation into first and second bone parts, the implant comprising: a median zone having a first end, a second end opposite the first end and defining an abutment, and a plurality of side faces between the first and the second ends converging toward the first end; a transition zone extending from the abutment and away from median zone; a first fixation zone extending from the transition zone and including first and second legs extending from the transition zone, the first and second legs defining a V-shaped gap extending from the transition zone, wherein the V shaped gap defines a first gap adjacent the transition zone and a second gap away from the transition zone, the first gap being less than the second gap; and a second fixation zone extending from the median zone.
 11. The intramedullary implant of claim 10, wherein the first end has a first cross-sectional dimension and the second end has a second cross-sectional section dimension, the first cross-sectional dimension being less than the second cross-sectional dimension.
 12. The intramedullary implant of claim 10, wherein the first end has a first width and the second end has a second width, the first width being less than the second width.
 13. The intramedullary implant of claim 10, wherein the first fixation zone extends from the first end and the second fixation zone extends from the second end.
 14. The intramedullary implant of claim 10, wherein the second fixation zone defines an opening therethrough.
 15. The intramedullary implant of claim 10, wherein the median zone includes an intermediate face between the plurality of side faces and the abutment.
 16. The intramedullary implant of claim 15, wherein the intramedullary implant defines a longitudinal axis and the intermediate face is parallel to the longitudinal axis.
 17. An intramedullary implant for implantation into first and second bone parts, the implant comprising: a generally triangular median zone having a first end and a second end, the first end having a first width; a first fixation zone extending from the first end of the median zone and including a plurality of legs; and a second fixation zone extending from the median zone, wherein the first width is greater than widths of the first fixation zone and the second fixation zone.
 18. The intramedullary implant of claim 17, wherein the first end defines an abutment.
 19. The intramedullary implant of claim 17, wherein the first end has a first cross-sectional dimension and the second end has a second cross-sectional section, the first cross sectional dimension being greater than the second cross-sectional dimension. 